Matthew Bracher-Smith

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Machine learning for genetic prediction of psychiatric disorders: a systematic review

V. Escott-Price, Matthew Bracher-Smith, Karen Crawford, 2020, Molecular Psychiatry.

Fractional anisotropy of the uncinate fasciculus and cingulum in bipolar disorder type I, type II, unaffected siblings and healthy controls

K. Tansey, X. Caseras, S. Foley, 2018, The British Journal of Psychiatry.

Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank

M. Owen, M. O’Donovan, J. Walters, 2022, Schizophrenia Research.

Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank

M. Owen, M. O’Donovan, J. Walters, 2022, Schizophrenia Research.

Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance

M. Owen, R. Anney, X. Caseras, 2022, Biological psychiatry global open science.

Age-dependent effect of APOE and polygenic component on Alzheimer's disease

Julie Williams, V. Escott-Price, G. Menzies, 2020, Neurobiology of Aging.

Association of Rare Copy Number Variants With Risk of Depression

G. Kirov, M. Owen, M. O’Donovan, 2019, JAMA psychiatry.

The Duffy-null genotype and risk of infection

T. Werge, M. Owen, M. O’Donovan, 2020, Human molecular genetics.

Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits

G. Kirov, M. Owen, M. O’Donovan, 2019, JAMA psychiatry.

Effects of pathogenic CNVs on biochemical markers: a study on the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, bioRxiv.

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2018, Journal of Medical Genetics.

Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank

G. Kirov, K. Murphy, X. Caseras, 2020, The British Journal of Psychiatry.

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, The British Journal of Psychiatry.

Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank

M. Owen, M. O’Donovan, Danny J. Smith, 2021, PloS one.

Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort

R. Anney, A. Pocklington, N. Bray, 2020, Translational Psychiatry.

Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, Molecular Psychiatry.

The role of rare copy number variants in depression

G. Kirov, M. Owen, M. O’Donovan, 2018, bioRxiv.

Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis

V. Escott-Price, D. Salih, J. Hardy, 2022, Neurobiology of Aging.

Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach

Peter Holmans, Andreas Artemiou, Andrew Pocklington, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review

V. Escott-Price, D. Ivanov, Matthew Bracher-Smith, 2021, Brain communications.

Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability

Sergio Marco Salas, V. Escott-Price, F. L. Raymond, 2022, medRxiv.

Pathway-specific polygenic scores for Alzheimer’s disease are associated with changes in brain structure in younger and older adults

P. Holmans, X. Caseras, V. Escott-Price, 2023, Brain communications.

Menopause age, reproductive span and hormone therapy duration predict the volume of medial temporal lobe brain structures in postmenopausal women

X. Caseras, J. Steventon, Matthew Bracher-Smith, 2023, Psychoneuroendocrinology.

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2018, Journal of Medical Genetics.

Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach

Sergio Marco Salas, V. Escott-Price, F. L. Raymond, 2023, Molecular Autism.

Menopause age, reproductive span and hormone therapy duration predict the volume of medial temporal lobe brain structures in postmenopausal women

X. Caseras, J. Steventon, Matthew Bracher-Smith, 2023, Psychoneuroendocrinology.

Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, Molecular Psychiatry.

Transcriptomics and weighted protein network analyses of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease

Matthew Bracher-Smith, Patrick A. Lewis, Valentina Escott-Price, 2024, NPJ Parkinson's disease.

Transcriptomics and weighted protein network analysis of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease

V. Escott-Price, C. Manzoni, Matthew Bracher-Smith, 2024, bioRxiv.

Fractional anisotropy of the uncinate fasciculus and cingulum in bipolar disorder type I, type II, unaffected siblings and healthy controls

K. Tansey, X. Caseras, Matthew Bracher-Smith, 2023 .